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威尔基综合征与假性胡桃夹综合征:一种罕见的组合——病例报告

Wilkie Syndrome and Pseudo-Nutcracker Syndrome a Rare Combination: Description of a Case.

作者信息

Farina Renato, Vasile Tiziana, Foti Pietro V, Pennisi Isabella, Basile Antonio

机构信息

Radiodiagnostic and Radiotherapy Unit, Department of Medical and Surgical Sciences and Advanced Technologies "GF Ingrassia", Istituto di Catania, Catania, ITA.

出版信息

Cureus. 2021 Oct 8;13(10):e18612. doi: 10.7759/cureus.18612. eCollection 2021 Oct.

Abstract

Wilkie's syndrome is a very rare vascular alteration caused by congenital or acquired reduction of space between the superior mesenteric artery (SMA) and aorta. In acquired form, it is caused by perivascular adipose tissue reduction due to rapid weight loss and, if symptomatic, causes postprandial vomiting and weight loss. The left renal vein (LRV) when it has a retro-aortic course can be compressed in aorto-vertebral space (AVS); if the stenosis is severe it can cause venous congestion symptoms with left flank pain, microhematuria, and thrombosis, this vascular alteration is known as a pseudo-nutcracker syndrome. The combination of Wilkie's and pseudo-nutcracker's syndrome (PNCS) is very rare and has not yet been described in the literature. We describe a case of a 62-year-old woman who presented symptoms and alterations typical of two syndromes.

摘要

威尔基综合征是一种非常罕见的血管病变,由先天性或后天性肠系膜上动脉(SMA)与主动脉之间间隙减小所致。后天性形式是由于体重快速减轻导致血管周围脂肪组织减少引起的,若出现症状,则会导致餐后呕吐和体重减轻。左肾静脉(LRV)走行于主动脉后方时,可在主动脉-椎体间隙(AVS)受压;若狭窄严重,可导致静脉淤血症状,伴有左侧腰痛、镜下血尿和血栓形成,这种血管病变被称为假性胡桃夹综合征。威尔基综合征和假性胡桃夹综合征(PNCS)的合并情况非常罕见,文献中尚未见描述。我们报告一例62岁女性病例,其出现了两种综合征的典型症状和病变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/910d/8579486/93b8e815b47f/cureus-0013-00000018612-i01.jpg

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